Muscle Protein Breakdown (MPB) is the catabolic physiological process involving the degradation of muscle tissue proteins into their constituent amino acids, which are then released into the circulation. While a basal level of MPB is necessary for muscle remodeling and repair, an excessive rate, particularly one exceeding the rate of muscle protein synthesis, leads to a net loss of muscle mass, a condition known as sarcopenia. This imbalance is critically influenced by hormonal status, nutrition, and physical activity.
Origin
This term is foundational to exercise physiology, nutritional science, and endocrinology, defining one half of the dynamic protein turnover process in skeletal muscle. The clinical significance became paramount with the understanding of catabolic states, such as those induced by high cortisol levels, prolonged fasting, or chronic illness. Research in this area is key to developing strategies for preserving lean body mass.
Mechanism
MPB is primarily mediated by the ubiquitin-proteasome system and lysosomal proteases, which are activated by catabolic signals. Glucocorticoids, such as cortisol, are potent inducers of MPB by increasing the expression of genes encoding these proteolytic enzymes. Conversely, anabolic hormones like insulin and testosterone suppress these pathways while simultaneously promoting muscle protein synthesis, illustrating the tight hormonal regulation of muscle mass homeostasis.
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